Heterogeneity in Slow Synaptic Transmission Diversifies Purkinje Cell Timing

The cerebellum plays an important role in diverse brain functions, ranging from motor learning to cognition. Recent studies have suggested that molecular and cellular heterogeneity within cerebellar lobules contributes to functional differences across the cerebellum. However, the specific relationship between molecular and cellular heterogeneity and diverse functional outputs of different regions of the cerebellum remains unclear. Here, we describe a previously unappreciated form of synaptic heterogeneity at parallel fiber synapses to Purkinje cells in the mouse cerebellum (both sexes). In contrast to uniform fast synaptic transmission, we found that the properties of slow synaptic transmission varied by up to threefold across different lobules of the mouse cerebellum, resulting in surprising heterogeneity. Depending on the location of a Purkinje cell, the time of peak of slow synaptic currents varied by hundreds of milliseconds. The duration and decay time of these currents also spanned hundreds of milliseconds, based on lobule. We found that, as a consequence of the heterogeneous synaptic dynamics, the same brief input stimulus was transformed into prolonged firing patterns over a range of timescales that depended on Purkinje cell location.

The properties of Purkinje cells, the output neurons of the cerebellar cortex, vary across regions, e.g., with respect to dendritic integration (Eccles et al., 1967), firing patterns (Zhou et al., 2014(Zhou et al., , 2015)), and axonal output (Voogd, 2011).However, the potential heterogeneity of Purkinje cell inputs is not well explored.
The cerebellar cortex is patterned into parasagittal microzones of Purkinje cells that are defined by their connectivity and correlate with their molecular identity (Cerminara et al., 2015).The glycolytic enzyme aldolase C or zebrin II is a wellinvestigated marker of Purkinje cell heterogeneity, which patterns the cerebellar cortex into parasagittal zebra-like bands (Apps et al., 2018).Zebrin bands receive similar input information and send similar output information (Sugihara and Shinoda, 2004;Voogd and Ruigrok, 2004;Pijpers et al., 2006;Apps and Hawkes, 2009;Ruigrok, 2011), although functional units within the cerebellum can also cross zebrin boundaries (Graham and Wylie, 2012).Zebrin identity correlates with some forms of molecular heterogeneity, including components of the metabotropic glutamate receptor 1 (mGluR1) signaling cascade (Mateos et al., 2001;Furutama et al., 2010;Wu et al., 2019).These molecular differences in Purkinje cells with different zebrin identities have been previously shown to correlate with differences in firing rate (Zhou et al., 2014) and with plasticity at PF synapses (Wadiche and Jahr, 2005).
Here, we tested the hypothesis that slow synaptic transmission at PF synapses varies across different lobules of the cerebellum.To do so, we measured synaptic currents at PF inputs to Purkinje cells in acute mouse brain slices.We found that the properties of slow synaptic currents varied up to threefold across different cerebellar lobules.As a consequence, PF inputs were transformed into a diverse range of prolonged firing outputs that depended on Purkinje cell location.This previously unappreciated heterogeneity in slow synaptic transmission thus diversifies Purkinje cell firing dynamics.

Materials and Methods
All experiments were done in accordance with the policies of the Canadian Council on Animal Care, using protocols approved by the Montreal General Hospital Facility Animal Care Committee, using C57BL/6J mice of both sexes from the Jackson Laboratory (Strain number 000664).
Purkinje cells were visualized under an Olympus BX61WI upright microscope using differential interference contrast optics.Patch electrodes (3-6 MΩ) were pulled from borosilicate glass and filled with an internal solution containing either one of the two recipes for both voltage and current-clamp experiments [containing the following (in mM): Recipe 1, 135 potassium gluconate, 7 NaCl, 2 MgATP, 0.3 NaGTP, 10 HEPES, 0.5 EGTA,10 phosphocreatine di(tris) salt (pH 7.2); Recipe 2, 128 potassium gluconate, 4 KCl, 10 HEPES, 10 sodium creatine phosphate, 4 MgATP, 0.3 NaGTP (pH 7.3)].Recordings made with the two internal solutions were identical and have been merged.For the experiments in Extended Data Figure 6-1, the internal solution contained 10 mM EGTA and 1 mM BAPTA with modifications to Recipe 1 containing (in mM) 130 potassium gluconate, 1 BAPTA, 7 NaCl, 2 MgATP, 0.3 NaGTP, 10 HEPES, 10 EGTA, and 10 phosphocreatine di(tris) salt (pH 7.2).For cell-attached recordings, the recording electrode was filled with NaCl (162.5 mM) solution (Perkins, 2006).Stimulation of the parallel fibers was performed using bipolar stimulating electrodes made from theta glass that were positioned in the outer molecular layer to trigger a slow EPSC or increase in firing.aCSF contained 50 µM picrotoxin and 5 µM NBQX for all recordings (except for Extended Data Fig. 1-1, where only picrotoxin was added, and Fig. 10, where no blockers were added).All whole-cell patch-clamp recordings were performed at 29-30°C.For cell-attached recordings, the temperature was maintained at 33 ± 1°C.Signals were acquired using a MultiClamp 700B amplifier at 10-100 kHz for the slow EPSC and 50 kHz for spiking experiments.The slow EPSC traces were averaged and filtered using a Bessel (eight-pole) filter with a low-pass filter of 1 kHz.Only recordings with series resistance <25 MΩ were included.Both input and series resistance were monitored for stability and discarded if they changed >20%.Slow EPSCs were elicited using 10 PF stimulation at 100 Hz for all experiments except Figures 3, 4, 9 and 10, where the frequency and number of PF stimulation were varied, as described in the figure legends.For voltage-clamp recordings, the cells were held at −70 mV.For the whole-cell spiking experiments (Fig. 9a-i), the slow EPSC traces were first recorded in voltage-clamp configuration and consequently switched to current-clamp with sufficient current injection to keep the cells below the threshold for spiking (between -49 and −57 mV at baseline.In only one flocculus cell was the cell spiking during the pre-stimulus baseline).For Figures 3 and 4, some cells that contributed to the data came from the same cells recorded in Figures 1, 9a-i, or 5. Cell-attached recordings were analyzed by normalizing the instantaneous firing frequency according to the following equation: (Inst.Freq.− Mean baseline Inst.Freq.) / (Inst.Freq.+ Mean baseline Inst.Freq.).
Fixed tissue preparation and immunofluorescence.Sedated mice underwent intracardial perfusion with ice-cold PBS followed by 4% PFA in PBS.Brains were postfixed in a 4% PFA solution at 4°C overnight.Subsequently, agarose-embedded cerebella were cut into 50 μm slices, in either a sagittal or coronal orientation, using a Vibratome 1000 Plus.For immunofluorescent labeling, slices were incubated with primary antibodies for 2 d at 4°C followed by secondary antibody incubation for 90-120 min at room temperature.Blocking of endogenous immunoglobulins with Fab fragment antibodies was performed when using mouse primary antibody.For immunostaining of 300-µm-thick slices, post-electrophysiology, and dye-fill (Fig. 2e-g), the slices were fixed in PFA for 1 to 4 h.The immunostaining protocol was the same as for 50 µm slice staining except for a 3 d incubation time with primary antibody (Table 1).
For Figures 2d and 8, prior to staining, slices were subjected to an antigen retrieval procedure, in which the slices were boiled at 90°C for 10 min in 10 mM trisodium citrate buffer (pH 8.5), followed by a 20 min cooldown period.For Figures 2, a, b, c, e, and g, and 8, blocking was performed in 1× PBS, pH 7.4, 0.4% Triton X-100, 5% BSA, and 0.05% sodium azide.For Figure 2d, 5% BSA was substituted with 8% heat-inactivated NGS.
Primary and secondary antibodies (Table 1) were diluted in the respective blocker solutions.
Epifluorescence images were captured on two different microscopes.Either we used a fully automated epifluorescence microscope system (Ti2-E, Nikon), equipped with a multispectral LED light source (SpectraX, Lumencor) and 10× Plan Apo 0.45 NA objective, a motorized emission filter wheel (HS-1025, FLI), a motorized stage, and an sCMOS camera (ORCA Fusion BT, Hamamatsu) controlled by Nikon Elements AR.Images were acquired as single images or as multipoint images that were stitched together using Nikon Elements AR's "large image" feature.Alternatively, images were acquired on an Olympus FV1000 laser scanning microscope, with a 20× or 40× lens, and acquired using Fluoview software (Olympus).Post-patch-clamp recording zebrin labeling was quantified by taking a ratio of fluorescent intensity within the Purkinje cell to the background fluorescence in the neighboring granule cell layer using Fiji (ImageJ).Only cells with a ratio >2 were considered zebrinpositive.Those with a ratio <1.7 were considered zebrin-negative, and those in between were considered uncertain and were therefore not included in the analysis shown in Figure 2.
Quantitative reverse transcription polymerase chain reaction (qRT-PCR).Cerebella of 26-33-day-old mice of both sexes were extracted in ice-cold aCSF bubbled with 95% O 2 and 5% CO 2 , with lobules of interest (lobules IV/V, lobule X, and flocculus) dissected under a dissection microscope and immediately snap frozen.Each biological sample was prepared by clubbing the lobule of interest from three mice.RNA extraction was performed using the RNeasy Mini Kit (Qiagen, 74104) following the manufacturer's instructions.RNA was then transcribed into cDNA using the QuantiTect Reverse Transcription Kit (Qiagen, 205313).qPCR was performed on a StepOnePlus Real-Time PCR System (Applied Biosystems by Thermo Fisher Scientific) using Fast SYBR Green Master Mix (Applied Biosystems, 4385612).Relative expression levels of each target transcript were determined by the ΔΔCт method (Livak and Schmittgen, 2001) using RPL13 mRNA levels as a reference.qPCR reactions were run as technical triplicates in 10 μl reactions (96-well format).The thermal cycling was performed with the following settings: holding stage, 20 s at 95°C; and cycling stage, 40 cycles of 3 s at 95°C and 30 s at 62°C.Melt curves were generated by heating from 62°C to 95°C at a temperature increment of 0.3°C.Primer sequences.A list of primer sequences is presented in Table 2.
Statistical analysis.Slice physiology data were analyzed in pCLAMP 11 (Clampfit), and the statistical tests were performed using GraphPad Prism, IBM SPSS, or the language R, except for Levene's test, which was performed on the JASP statistics program.
The data were tested for normality using the Shapiro-Wilk test and for equality of variances using Levene's test.If the data were normally distributed and had equal variances, then it was analyzed using ordinary one-way ANOVA followed by Tukey's multiple-comparisons test.If either one of the assumptions was violated, the Kruskal-Wallis test followed by Dunn's multiple-comparisons test was used.For paired comparisons, paired t tests were used if the data passed the normality test using the Shapiro-Wilk test.If not, the Wilcoxon matched-pair signed rank test was used.For Extended Data Figure 1-1, an unpaired t test was used following the normality check using the Shapiro-Wilk test.
In several experiments, more than one cell came from a single mouse.Therefore, we fitted a linear mixed-effects (LME) model (both in SPSS and R) with the mouse as a random effect for the fixed effect of each variable we assessed (Yu et al., 2022).Even when accounting for more than one cell coming from a single mouse, analysis of data in Figure 1 demonstrates that the peak amplitude is significantly different across lobules, with a Bonferroni's pairwise comparison indicating a significant difference between lobules IV/V and lobule X (p < 0.05).In addition, the time of peak of all three lobules was also significantly different from each other (lobules IV/V vs flocculus and lobule X = p < 0.001; lobule X vs flocculus = p < 0.05).The half-width was also significantly different across lobules (pairwise comparison: lobules IV/V vs lobule X and  Neurosci., September 11, 2024 • 44(37):e0455242024 • 3 flocculus = p < 0.001; lobule X vs flocculus = p < 0.01).Thus, the heterogeneity in sEPSCs held true even when accounting for the effect of mouse identity.We tried to fit LME models to all datasets in the paper, but only in a subset of figures was the LME able to estimate a random effect coming from the mouse identity.Importantly, in no case did the LME contradict any of the significant effects we describe.Details on statistical analysis are provided in each figure legend, with additional information in Extended Data Table 1.
Single-nucleus RNA-seq analysis.The processed single-cell RNA-seq data from Kozareva et al., 2021 was filtered to contain only the 16,634 Purkinje cells using Seurat 5.0.1 in R 4.3.2.The slots containing metadata, raw counts, normalized, and scaled data were copied from the author's Seurat 2.3.4 object found here https://singlecell.broadinstitute.org/single_cell/study/SCP795/a-transcriptomic-atlas-of-the-mousecerebellum to create a new Seurat v5 compatible object.Variable features, principal components, and UMAP dimension reductions were then recalculated using the respective Seurat functions on the Purkinje-only data.Plots were produced using the DimPlot and DotPlot functions of Seurat and ggplot2.Differential gene expression analysis was performed using the FindMarkers function of Seurat.To determine if genes were differentially expressed between lobules, the Seurat function FindMarkers with default parameters (Wilcoxon rank sum test with Bonferroni's correction for multiple tests) was used pairwise between the three lobes/regions of interest on all detected genes.Genes with an adjusted p-value < 0.05 were deemed to be significantly differentially expressed between tested lobes.

PF-driven slow EPSCs were heterogeneous across cerebellar lobules
A remarkable feature of the cerebellar cortex is its stereotypical anatomy, composed of well-defined regions and lobules that can be reproducibly identified.However, it remains unclear whether Purkinje cells in different cerebellar regions and lobules show uniform or distinct synaptic properties and how this may contribute to region or lobule-specific cerebellar cortex output.To help resolve this, we compared the physiological properties of slow EPSCs at Purkinje cells in lobules located in the midline vermis with those in the laterally positioned floccular lobule (Fig. 1a), regions that have different functional roles (Witter and De Zeeuw, 2015a) and molecular profiles (Fujita et al., 2014).We measured PF-driven slow EPSCs using patch-clamp recordings from Purkinje cells (see Materials and Methods) in different lobules of the cerebellum taken from acute mouse brain slices (Fig. 1b).The slow EPSC at PF to Purkinje cell synapses was measured in response to physiologically relevant high-frequency PF stimulation in the presence of antagonists of AMPARs and GABA A (γ-amino butyric acid A) receptors (50 µM picrotoxin, 5 µM NBQX; Batchelor and Garthwaite, 1997;Brasnjo and Otis, 2001;Canepari et al., 2004;Chadderton et al., 2004;Jorntell and Ekerot, 2006;van Beugen et al., 2013;Hartmann et al., 2008).
We found that slow EPSCs in vermal lobules IV/V had dynamics surprisingly different from those in the flocculus (Fig. 1b-d).In particular, the time of peak of lobules IV/V slow EPSCs was up to threefold lower than the time of peak of floccular slow EPSCs (Fig. 1d).Moreover, slow EPSCs in lobules IV/V were less variable than those in the flocculus (Fig. 1d,e).Next, we measured slow EPSCs from lobule X of the vermis.Lobule X is similar to the flocculus in terms of being largely zebrin-positive, in contrast to the largely zebrin-negative lobules IV/V.We found that the times of peak of slow EPSCs in lobule X were similar to those in the flocculus and more delayed than those in lobules IV/V (Fig. 1d).Purkinje cells in lobule X, like those in the flocculus, displayed heterogeneous timing of their slow current events (Fig. 1d,e).The heterogeneity we observed in slow EPSC dynamics was also reflected by slower decay times and longer halfwidths in vermal lobule X and the flocculus, compared with vermal lobules IV/V (Fig. 1f,g).In addition, the slow EPSC had a slightly lower amplitude in lobule X, which aligned with previous findings (Fig. 1c; Wadiche and Jahr, 2005).Next, we measured how the size of the slow EPSC impacts its timing by comparing the peak amplitude versus the time of peak of each cell across the three lobules.Regardless of the peak amplitude of the slow EPSC in lobules IV/V, the time of peak had a low variance when compared with other lobules (Fig. 1h, pink).In marked contrast, slow EPSCs from the flocculus (Fig. 1h, blue) formed a nonoverlapping population with a delayed time of peak.Finally, slow EPSCs from lobule X (Fig. 1h, green) showed a time of peak in between these two populations but were distinguished by their longer decay times.Thus, Purkinje cells possess distinct timing and shape of slow EPSCs depending on their location in different lobules.
In contrast to the differences observed with the slow EPSCs, we could not detect a difference in the timing of fast EPSCs in lobules IV/V and the flocculus (Extended Data Fig. 1-1).Thus, the timing heterogeneity in slow EPSCs was specific to this current and was not a feature of the synapse or the cell.

Zebrin identity did not determine slow EPSC properties
The differences in slow EPSCs in lobules IV/V and the flocculus could be due to a variety of molecular and cellular signatures of Purkinje cells in these lobules.One molecular signature that distinguishes Purkinje cells with different properties is zebrin.It was previously shown that Purkinje cells in vermal lobules IV/V are largely zebrin-negative while those in vermal lobule X and the flocculus are largely zebrin-positive (Fujita et al., 2012;Fig. 2a-d).However, some Purkinje cells within these lobules do not follow the same zebrin identity as the majority of other Purkinje cells within the lobule.We took advantage of this intrinsic variability to interrogate how the zebrin identity of individual Purkinje cells relates to their slow EPSC timing.In order to do this, patch-clamp recordings from different regions were first performed, during which the recorded cell was dye-filled.Slices were subsequently fixed and immunolabelled retrospectively for zebrin (Fig. 2e,f).This way, the zebrin identities of individual cells were identified after characterizing their slow EPSCs.As expected, most cells in each region followed the zebrin identity of that lobule.However, as expected, instances were found where Purkinje cells had the opposite zebrin identity (Fig. 2g).Surprisingly, we found that the identity of the lobule rather than an individual Purkinje cell's zebrin identity defined the timing of the slow EPSC (Fig. 2g).For example, the sparse zebrin-positive Purkinje cells in lobules IV/V had slow EPSC currents that followed the relatively fast kinetics of the majority zebrin-negative cells within that region.A mirror effect was seen for Purkinje cells in the flocculus and lobule X, where sparse zebrin-negative cells showed slow EPSCs with kinetics similar to Purkinje cells that were zebrin-positive.Thus, our results show that cerebellar lobule rather than individual Purkinje cell zebrin expression determined slow EPSC properties.Parasagittal acute cerebellum slices were used for recordings in vermis lobules IV/V and X, while coronal sections were used for flocculus recordings.b, Representative sEPSC traces depict a delayed time of peak in lobule X and the flocculus compared with lobules IV/V.Scale bar, 100 pA, 500 ms.c, Peak amplitudes of sEPSCs were similar across lobules.*p < 0.05, Kruskal-Wallis analysis of variance on ranks followed by Dunn's multiple-comparisons test.d, sEPSC time of peak was earlier in lobules IV/V in comparison with lobule X and the flocculus.Kruskal-Wallis analysis of variance on ranks followed by Dunn's multiple-comparisons test (****p < 0.0001).e, High heterogeneity in the time of peak within lobule X and the flocculus compared with lobules IV/V is demonstrated by higher coefficients of variation.f, Lobule X sEPSCs exhibited the longest 90-10% decay time.Both lobule X and flocculus sEPSCs had longer decay times than those from lobules IV/V.*p < 0.05, ****p < 0.0001, Kruskal-Wallis analysis of variance on ranks followed by Dunn's multiple-comparisons test.g, A longer half-width sEPSC was observed in lobule X and the flocculus compared with lobules IV/V (****p < 0.0001, Kruskal-Wallis analysis of variance on ranks followed by Dunn's multiple-comparisons test).h, sEPSCs with similar peak amplitudes in lobules IV/V, lobule X, and the flocculus had different times of peak.Bubble size represents the decay time of the sEPSC.Data from each lobule were fit in an assumption-free manner with a spline in equivalent color.Violin plots show median and quartiles.(c-f, h: lobules IV/V = 56 cells from 41 mice, lobule X = 35 cells from 27 mice, flocculus = 23 cells from 14 mice.g: lobules IV/ V = 42 cells from 33 mice, lobule X = 33 cells from 26 mice, flocculus = 23 cells from 14 mice).Please refer to Extended Data Figures 1-1-1-3 for further information.Additional details on statistics are presented in Materials and Methods and Extended Data Table 1.Slow EPSC heterogeneity persisted across a range of parameters It is possible that the heterogeneity we observed is only present with the specific PF stimulation parameters we used (10 pulses at 100 Hz), which would limit its relevance.We ruled out this possibility by testing a range of parameters.We found that the heterogeneity in slow EPSCs remained even with a lower number of stimuli [starting with three pulses, shown to be the lowest number to activate mGluR1 (Brasnjo and Otis, 2001), and going up to five stimuli; Fig. 3a-i].In addition, we maintained the number of stimuli at 10 but tested a range of stimulation frequencies, from 50 to 200 Hz.Across all frequencies, the time of peak of the slow EPSC in lobules IV/V was early and highly homogeneous, in contrast to the delayed and varied time of peak in lobule X and the flocculus.In all cases, the decay was different across lobules in a manner similar to that described in Figure 1 (Fig. 4a-c).Thus, the specific number of stimuli or the frequency did not determine the heterogeneity in slow EPSCs.
We were concerned that the time after break-in for whole-cell patching could contribute to dialysis of the intracellular cytosol and impact pathways necessary for the slow EPSC (Sakmann and Neher, 1984;Rae and Fernandez, 1988;Cahalan and Neher, 1992).To account for this, we analyzed a subset of Purkinje cells from Figure 1 in which slow EPSCs were measured within the restricted time window of 10-20 min after break-in.The results showed that even within this restricted subset of cells, the heterogeneity observed across lobules remained (Extended Data Fig. 1-2).
Recent studies describe sex-based differences in cerebellar structure and physiology (Mercer et al., 2016;Steele and Chakravarty, 2018).To test this possibility, we compared slow EPSCs from male and female mice.We found no difference between the slow EPSC properties of Purkinje cells from male and female mice (Extended Data Fig. 1-3).

Heterogeneity in mGluR1-TRPC3 signaling may contribute to Purkinje cell slow EPSCs
The slow EPSC was previously shown to depend on mGluR1 (Hartmann et al., 2008).We wondered if the heterogeneity of the slow EPSC that we found relied on other types of signaling across the different lobules.However, we found that the noncompetitive mGluR1 antagonist CPCCOEt (100 µM; Hartmann et al., 2008) blocked slow EPSCs in all three regions (Fig. 5a), arguing against this possibility.Downstream of mGluR1, the slow EPSC is mediated by the nonselective cation channel TRPC3 (Hartmann et al., 2008;Chae et al., 2012;Cole and Becker, 2023).To test how TRPC3 blockade impacts the time of peak, we used the tyrosine kinase inhibitor genistein (100 µM; Vazquez et al., 2004;Y. Kim et al., 2012b) and the TRPC channel blocker SKF96365 (10 µM; Chae et al., 2012;Song et al., 2014;Cole and Becker, 2023), which both partially block the slow EPSC, allowing us to measure the kinetics of the remaining current.We found that the magnitude of the slow EPSC was consistently reduced by genistein and by SKF96365 across lobules, but there was no shift in timing that could explain the differences between lobules (Fig. 5b-e).
The characteristically prolonged time course of the slow EPSC is related to the associated G-protein-dependent signaling cascade (see Fig. 6a for a noncomprehensive schematic; Hartmann et al., 2011;Kano and Watanabe, 2017;Hirai and Kano, 2018;Cole and Becker, 2023).However, the signaling pathways connecting mGluR1 and TRPC3 signaling, and its regulation, are not fully understood (Cole and Becker, 2023).Despite this, we wanted to identify candidate molecular players underlying the diversity of slow EPSCs across lobules.Therefore, we performed a bioinformatic analysis of Purkinje cell transcriptomes using a published single-nucleus RNA sequencing dataset (Kozareva et al., 2021).We separated Purkinje cell transcriptomes by lobule of interest and focused on molecular candidates related to the mGluR1-TRPC3 pathway (Fig. 6b; Hartmann et al., 2011;Kano and Watanabe, 2017;Hirai and Kano, 2018;Cole and Becker, 2023).Comparison of gene expression demonstrated statistically significant differences across lobules.Key features of our analysis aligned with previous findings.For instance, the expression of Grm1, which encodes mGluR1, was greater in lobules IV/V than in the flocculus and lobule X.This is consistent with greater mGluR1b in zebrinnegative zones (Mateos et al., 2001).TRPC3 expression was also greater in the largely zebrin-negative lobules IV/V, in contrast to the largely zebrin-positive flocculus and lobule X.This is consistent with previous studies, although it is also known that TRPC3 expression does not perfectly overlap with zebrin zones (Wu et al., 2019).
We then focused our analysis on the molecules that distinguish regions with slow timing (lobule X and flocculus) from regions with fast timing (lobules IV/V).We found that there were several differences in gene expression, including in the following: (1) Prkcg, encoding PKCγ (protein kinase C γ); (2) Plcb1 and 4, encoding PLCβ (phospholipase C-β); (3) Dgkg, encoding DAG kinase γ; and (4) Gabbr2, encoding GABA B (γ-aminobutyric acid type B) receptors.In addition, Grid, encoding GluD2 (glutamate receptor delta) channels, had lower expression in lobule X relative to the other two regions (see Discussion).Finally, stromal interaction molecule STIM1 is a key controller of mGluR1-dependent synaptic transmission and differs between lobules IV/V versus lobule X and the flocculus.However, it is also different between the two regions that both have slow timing, lobule X and the flocculus.Thus, we identified more than one molecular correlate of heterogeneity across lobules, within known components of mGluR1-TRPC3 signaling pathways.In addition, these signaling components are likely to interact with each other (Cole and Becker, 2023).Moreover, our bioinformatic analysis by separating cells from different lobules obscures the within-lobule heterogeneity observed both in previous studies of the Purkinje cell transcriptome (Kozareva et al., 2021) and in our data.Overall, we found several key differences in the signaling pathways that could mediate slow EPSC heterogeneity across lobules.
Analyzing their single-cell RNA-seq dataset of cerebellar Purkinje cells, Kozareva et al. (Kozareva et al., 2021) describe nine molecularly defined clusters that could be separated by zebrin identity: two clusters of zebrin-negative cells and seven clusters of zebrin-positive cells.We examined the transcriptomic profiles of Purkinje cells from the three lobules that we are interested in, in terms of these nine clusters (Fig. 6c).Surprisingly, lobular clusters do not fully align with the clusters defined by gene cells were zebrin-positive (green hollow circles).However, even zebrin-positive cells (green hollow circles) in lobules IV/V had a characteristically shorter time of peak, and zebrin-negative cells (black hollow circles) in lobule X and the flocculus had a delayed time of peak.(g: lobules IV/V = 37 cells from 28 mice, lobule X = 22 cells from 18 mice, flocculus = 15 cells from 14 mice).
Thomas et al. • Synaptic Heterogeneity in Purkinje Cells expression pattern (Fig. 6d,e), and the three regions we investigated fall into separate clusters.This observation may serve to explain the large amount of heterogeneity that we found across single cells.It also suggests that there is high-dimensional transcriptomic heterogeneity within and across regions of the cerebellum.
Next, we assessed whether and how buffering intracellular calcium might affect the heterogeneity of timing of the slow EPSC.However, heterogeneity in slow EPSC timing persisted in recordings performed with 10 mM EGTA and 1 mM BAPTA in the internal solution, demonstrating that, at least at these concentrations, there is no effect on the heterogeneity in timing (Extended Data Fig. 6-1).
While the heterogeneity in the signaling pathway connecting mGluR1 to TRPC3 can explain the heterogeneity in slow EPSC we observe, it has also been shown that TRPC3 itself has different b, e, h: lobules IV/V = 5 cells from 3 mice, lobule X = 7 cells from 3 mice, flocculus = 10 cells from 5 mice.c, f, i: lobules IV/V = 5 cells from 3 mice, lobule X = 7 cells from 3 mice; flocculus = 11 cells from 5 mice).Additional details on statistics are in Extended Data Table 1.
splice variants (Y.Kim et al., 2012b).The distribution of splice variants across lobules in the cerebellum has not, to our knowledge, been previously investigated.Therefore, in order to further investigate the splice variants of the receptor and channel mediating the slow EPSC, we performed quantitative reverse transcription-PCR analysis.We separated lobules IV/V and X of the vermis, as well as the flocculus, extracted RNA, and tested the relative abundance of mGluR1, TRPC3, and their splice variants (Fig. 7a-f).Lobules IV/V showed higher expression levels of mGluR1b when compared with lobule X and the flocculus, which agrees with published differences in the isoforms of mGluR1 across zebrin-positive versus negative regions (Mateos et al., 2001).Surprisingly, we also found a difference between the expression of the splice variants of TRPC3, TRPC3c, and 3b (Y.Kim et al., 2012b).TRPC3c showed increased expression in lobules IV/V, the region with fast kinetics, compared with lobule X and the flocculus.In agreement with previous literature showing an anticorrelation between the expression levels of TRPC3 and zebrin across lobules (Wu et al., 2019), the expression of total TRPC3 was also higher in lobules IV/V.Taken together, our results identified a correlation between the expression levels of the splice variants TRPC3c and mGluR1b and shorter versus longer dynamics of the slow EPSC.Previously, it has been shown that mGluR1 and TRPC3 are localized in the molecular layer, where the Purkinje cell dendritic tree and parallel fiber synapses are (Grandes et al., 1994;Wu et al., 2019).In order to confirm that this is true across the lobules we analyzed, mGluR1a [which is distributed through all lobules (Grandes et al., 1994;Yamasaki et al., 2021)] and TRPC3 were visualized across lobules using antibody staining.As expected, immunofluorescence signals for both mGluR1 and TRPC3 were present in Purkinje cells and throughout their dendritic tree in the molecular layer in all three regions (Fig. 8a,b).Moreover, the ratio of fluorescence intensity of TRPC3 to mGluR1a was higher in lobules IV/V than in lobule X and the flocculus, which is consistent with the higher TRPC3 seen in zebrin-negative regions (Wu et al., 2019) and with our RT-qPCR data (Fig. 8c)., 75, 100, 125, 150, and 200 Hz.**p < 0.01, Kruskal-Wallis test followed by Dunn's multiple-comparisons test.b, From left to right, sEPSC time of peak is earlier in lobules IV/V in comparison with lobule X and the flocculus, in response to 10 PF stimulations at 50, 75, 100, 125, 150, and 200 Hz.****p < 0.0001, Kruskal-Wallis test followed by Dunn's multiple-comparisons test.c, From left to right, Time for the sEPSC peak amplitude to decay from 90 to 10% was longer for both lobule X and the flocculus in comparison with lobules IV/V, in response to 10 PF stimulations at 50,75,100,125,150,and 200 Hz. 50 Hz,75 Hz *p < 0.05, ****p < 0.0001, Kruskal-Wallis test followed by Dunn's multiple-comparisons test.100-200 Hz ***p < 0.001, ****p < 0.0001, ordinary one-way ANOVA followed by Tukey's multiple-comparisons test.In order to compare the effect of PF stimulation frequency on the sEPSC, the 100 Hz dataset included a subset of the cells that contributed to Figure 1, as well as to Figure 9. Violin plots show median and quartiles.(50 Hz: lobules IV/V = 24 cells from 18 mice, lobule X = 17 cells from 17 mice, flocculus = 8 cells from 6 mice; 75 Hz: lobules IV/V = 26 cells from 18 mice, lobule X = 17 cells from 17 mice, flocculus = 8 cells from 6 mice; 100 Hz: lobules IV/V = 28 cells from 18 mice, lobule X = 17 cells from 17 mice, flocculus = 8 cells from 6 mice; 125 Hz: lobules IV/V = 25 cells from 18 mice, lobule X = 17 cells from 17 mice, flocculus = 8 cells from 6 mice; 150 Hz: lobules IV/V = 25 cells from 17 mice, lobule X = 17 cells from 17 mice, flocculus = 8 cells from 6 mice; 200 Hz: lobules IV/V = 24 cells from 16 mice, lobule X = 16 cells from 16 mice, flocculus = 8 cells from 6 mice).Additional details on statistics are in Extended Data Table 1.
Slow EPSC heterogeneity diversifies the timing of Purkinje cell firing Next, we wondered how the slow EPSC heterogeneity would impact Purkinje cell spiking.It is known that the firing properties of Purkinje cells in response to depolarization are not uniform across the cerebellum (C.H. Kim et al., 2012a;Zhou et al., 2014).To explore this, cells were first recorded in voltageclamp configuration to measure the slow EPSC (Fig. 9a-c).Next, recordings were switched to current-clamp configuration, allowing Purkinje cells to fire action potentials in response to synaptic input (Fig. 9d-f).This allowed us to look directly at any relationship between slow EPSC timing and parallel fiber-evoked modulation of spiking.We uncovered a difference in the timing of the firing response across lobules that matched the slow EPSC kinetics.Lobules IV/V, which had faster EPSC kinetics, had an equivalently short firing response.In contrast, slow EPSCs in lobule X and the flocculus, which had a diversity of longer delays, triggered prolonged firing responses in comparison with the responses elicited in lobules IV/V (Fig. 9d-i).Table 1. 6. Heterogeneity in mGluR1-TRPC3 signaling, and in overall gene expression, in lobules IV/V, lobule X, and the flocculus.a, Schematic of the postsynaptic signaling pathway involved in the slow EPSC at PF to Purkinje cell synapses (combined and adapted from Hartmann et al., 2011;Kano and Watanabe, 2017;Hirai and Kano, 2018;Cole and Becker, 2023).b, Visualization of gene expression heterogeneity in single-nucleus RNA-seq data of 16,634 Purkinje cells, from Kozareva et al. (2021).The dot plot shows the scaled expression of selected genes of interest across cerebellar regions.The regions of interest are highlighted with appropriately colored boxes (Flocc = flocculus).The following transcripts code for the proteins of interest in b: Trpc3, TRPC3; Grm1, mGluR1; Itpr1, IP 3 receptor; Prkcg, PKCγ; Plcb, isoforms of PLCβ; Gabbr, GABA B receptor; Grid2, GluD2 receptor; Dgkg, DAG kinase isoforms; Pld1, phospholipase D1; Prkca, protein kinase C; Stim1, stromal interaction molecule 1. c, Visualization of gene expression heterogeneity in scRNA-seq data of 16,634 Purkinje cells as described by Kozareva et al. (2021).UMAP dimension reduction showing original authors' identified PC clusters.Aldoc and zebrin are equivalent.d, UMAP plot showing the region of the cerebellum that the cells were sampled from, demonstrating the lack of full alignment between molecularly defined cell-type and lobular identity.e, Lobules IV/V, lobule X, and the flocculus are separated out from d, demonstrating that all three regions fall in different clusters, with some overlap.Also see Extended Data Figure 6-1.
We were concerned that the potentially dialyzing effects of whole-cell recordings (Sakmann and Neher, 1984;Rae and Fernandez, 1988;Cahalan and Neher, 1992) affected our results.We also wondered what the effect of slow EPSC heterogeneity was on intrinsically firing cells.To address these concerns, we explored how slow EPSC heterogeneity affected Purkinje cell firing using cell-attached recordings.To isolate slow EPSC-driven effects, both AMPARs and GABA A receptors were blocked with 5 µM NBQX and 50 µM picrotoxin, as previously.We observed that different regions of the cerebellum showed heterogeneity in the timing of their firing response (Fig. 9j-l), which validated our previous whole-cell recordings (Fig. 9a-i).The enhancement of firing was brief in lobules IV/V, in comparison with the delayed and prolonged enhancement of firing in lobule X and the flocculus.
An important limitation of these data is that GABAergic inhibition is blocked, although fast inhibitory synaptic transmission is a major determinant of Purkinje cell firing.In addition, AMPAR-dependent fast synaptic transmission is also blocked, in order to visualize the time course of the mGluR1-dependent slow synaptic response.Therefore, in order to identify whether the heterogeneous responses to parallel fiber input across lobules hold true even in the presence of GABAergic inhibition and fast glutamatergic transmission, we performed cell-attached recordings in the absence of picrotoxin and NBQX.Cell-attached recordings were made from Purkinje cells in each of the three regions, lobules IV/V, lobule X, and the flocculus, while parallel fibers were stimulated five times at 100 Hz to trigger mGluR1dependent slow synaptic currents (Fig. 10a-c).As expected, the absence of a fast synaptic transmission block resulted in a more rapid response to stimuli across all three lobules.In addition, the absence of an inhibition block led to a more rapid return to baseline firing rate.However, the marked differences in response timings across the three lobules were still observed, with Purkinje cells in lobules IV/V showing a relatively short increase in firing rate compared with cells in lobule X and the flocculus (Fig. 10a-c).Thus, the heterogeneity in Purkinje cell responses remains true even under conditions where GABAergic inhibition and fast glutamatergic transmission are intact.
Taken together, our findings demonstrate that the same synaptic input led to an increase in firing rate over different timescales across lobules.Thus, the same synaptic input diversified PF-triggered responses heterogeneously across the cerebellum.1.

Discussion
Our study reveals how Purkinje cells in different locations of the cerebellum transform the same synaptic input into heterogeneous outputs that vary in timing and dynamics.The difference in slow EPSC timing across lobules of the cerebellum correlated well with components of the mGluR1-TRPC3 signaling pathway, implicating multiple molecular players in the regulation of slow synaptic signaling.Our results highlight a hitherto unappreciated form of cellular heterogeneity that complements and expands the known repertoire of cerebellar diversity (Cerminara et al., 2015).
Anatomical and molecular subdivisions of the cerebellum Architecturally, the cortex of the cerebellum consists of five transverse zones (Apps and Hawkes, 2009) and three longitudinal compartments, containing the folded lobules.Although individual lobules have been correlated with specific functions, the fissures between lobules do not necessarily demarcate functionally distinct circuits (Apps and Hawkes, 2009;Witter and De Zeeuw, 2015a).Functionally, the circuit between the inferior olive, the cerebellar cortex, and the deep cerebellar nuclei (and vestibular nucleus) is demarcated longitudinally into modules.Modules are thus defined by their connectivity and are further subdivided into microzones, which receive common climbing fiber input (reviewed by Apps et al., 2018).Another way to compartmentalize the cerebellar cortex consists of the parasagittal bands or stripes that demarcate differences in Purkinje cell molecular properties and information processing, most commonly described by zebrin identity (De Zeeuw, 2021).Of note, the zebrin identity of a parasagittal band of Purkinje cells correlates or anticorrelates with 126 different molecules (Rodriques et al., 2019), including signaling components of the mGluR1 pathway.Since both mGluR1 and TRPC3 are critical for cerebellar synapses to function normally and to undergo plasticity (Aiba et al., 1994;Yamakawa and Hirano, 1999;Ichise et al., 2000;Kishimoto et al., 2002;Knöpfel and Grandes, 2002;Hartmann et al., 2004Hartmann et al., , 2008;;Lüscher and Huber, 2010;Ohtani et al., 2014;Hartmann and Konnerth, 2015;Kano and Watanabe, 2017), the parasagittal location of a Purkinje cell has implications for how it processes information and how synapses onto it undergo long-term potentiation or LTD.It is also important to note that the alignment of mGluR1 signaling-related molecules and zebrin is not always exact.Generally, mGluR1b is present in complementary bands to zebrin (Mateos et al., 2001); the IP 3 receptor, which can modulate TRPC3 (Y.Kim et al., 2012b), is present in bands similar to zebrin, although not exactly overlapping (Furutama et al., 2010).PLCβ3 and PLCβ4 are expressed in mostly nonoverlapping bands, with PLCβ3 expression in zebrinpositive PCs, depending on location within the anteroposterior transverse zone, and PLCβ4 expression in zebrin-negative PCs (Sarna et al., 2006).TRPC3 itself is expressed in a roughly complementary fashion to zebrin (Wu et al., 2019).All of these molecules directly impact both baseline transmission and plasticity at  parallel fiber synapses.However, individual parallel fibers can extend across parasagittal Purkinje cell stripes (Apps et al., 2018), thereby carrying the same information to different microzones.

The role of zebrin
We assessed the relationship of our observations of Purkinje cell heterogeneity in light of zebrin-positive or zebrin-negative identity.However, as described above, rather than having just two possible types of molecular signature, Purkinje cells have diverse molecular properties (Guo et al., 2021;Kozareva et al., 2021).In addition, zebrin expression is also not necessarily binary, i.e., solely zebrin-positive or zebrin-negative but has been described as having graded expression (Fujita et al., 2014).A broad diversity of cellular properties would serve to expand the computational capacity of the cerebellum.Our analysis of Purkinje cell transcriptomes also supports this idea of diversity in multiple different interacting molecules.

Key molecular determinants of synaptic diversity
Our analysis of published Purkinje cell transcriptomes to investigate regional differences highlights several molecules that are differentially expressed in the lobules with different slow EPSC dynamics.There is an increase in Prkcg expression, which encodes PKCγ, in the region with faster slow EPSCs relative to the other two regions.As summarized in Figure 6a, PKCγ negatively regulates TRPC3, which would be consistent with a shorter or more tightly timed slow EPSC (Hartmann et al., 2011;Cole andBecker, 2023). Plcb1, 3, and4, encoding PLCβ (Hashimoto et al., 2001;Miyata et al., 2001), are also differentially expressed in lobules IV/V versus lobule X and the flocculus; lobule X and the flocculus also have different expression levels.Potentially, this could lead to faster activation of TRPC3 in lobules IV/V.In addition, Dgkg, encoding DAG kinase γ, is higher in lobules IV/V than in the other two regions.This is particularly interesting, as DAG-kinase has been shown to directly control the response duration of mGluR1 (Guo et al., 2021), which is consistent with our results.Grid2, encoding GluD2 channels, had a lower expression in lobule X relative to the other two regions.Since loss of GluD2 regulates mGluR1-TRPC3 signaling (Kato et al., 2012;Ady et al., 2014), this may contribute to the characteristically small-amplitude and long-decay sEPSCs in lobule X.Our analysis also showed that Gabbr2, encoding GABA B receptors, was expressed at a higher level in the regions with slow dynamics, i.e., lobule X and the flocculus, relative to the region with fast dynamics, lobules IV/V.GABA B receptors have been implicated in mGluR1-TRPC3 interactions and in the mGluR1-dependent slow EPSC, although the mechanisms by which it does so remain unknown (Tian and Zhu, 2018).Our comparison of lobular identity with previously described, transcriptionally defined categories of Purkinje cells also suggests a diversity of categories within a lobule (Fig. 6; Kozareva et al., 2021).Moreover, Kozareva et al. described greater heterogeneity in zebrin-positive clusters of Purkinje cells (Kozareva et al., 2021), an observation that correlates with the greater heterogeneity in slow EPSC properties that we see in the largely zebrinpositive lobule X and flocculus, in comparison with the relatively uniform slow EPSC properties in lobules IV/V.Our findings are also consistent with a recent study (Guo et al., 2021), which demonstrated diversification of timing in a cell-autonomous manner by mGluR1 signaling, in the context of cerebellar unipolar brush cells.

Heterogeneity of TRPC3 isoforms
Our results also demonstrated a correlation between increased expression of the splice variant TRPC3c and shorter slow EPSCs in lobules IV/V.TRPC3c is distinguished from TRPC3b by the loss of a single exon, which codes for a large part of the calmodulin-IP 3 receptor binding domain (Y.Kim et al., 2012b).Thus, it has altered intracellular regulation and sensitivity to Ca 2+ .In addition, there is an increased channel opening rate.However, the regulation and function of TRPC3 splice variants in Purkinje cells in vivo is not well understood, and it remains unclear how TRPC3c alone can directly cause faster sEPSCs (Hartmann et al., 2011;Nelson and Glitsch, 2012;Y. Kim et al., 2012b;Hartmann and Konnerth, 2015;Sierra-Valdez et al., 2018).Indeed, our results also demonstrate that there are additional molecular players that are likely to be responsible for different shapes and timing of the slow EPSC.Overall, our findings point to the necessity to more fully understand the expression and regulation of the mGluR1-TRPC3 cascade (Bodzęta et al., 2021;Cole and Becker, 2023) and highlight that previously undescribed regional heterogeneity in splice variants needs to be considered.

Implications for plasticity
Both mGluR1 and TRPC3 are essential for LTD at PF to Purkinje cell synapses (Aiba et al., 1994;Chae et al., 2012;S. J. Kim, 2013), and LTD is critical for behavioral learning (Suvrathan et al., 2016;Suvrathan and Raymond, 2018;De Zeeuw et al., 2021).However, LTD is directly dependent on the postsynaptic Ca 2+ signal (Wang et al., 2000;Ito, 2001).The slow EPSC and the Ca 2+ signal are thought to be two independent intracellular signaling cascades downstream of mGluR1 (Takechi et al., 1998;Hartmann et al., 2011;Hartmann and Konnerth, 2015;Ouares and Canepari, 2020).Therefore, the timing of the slow EPSC is likely not related to the timing requirements for plasticity.However, it remains unclear how the diverse response timings of TRPC3 interact with heterogeneous plasticity mechanisms across the cerebellum, such as the demarcation into upbound and downbound zones (De Zeeuw, 2021).

The link to Purkinje cell firing patterns
The slow EPSC-driven heterogeneity in firing we describe here adds to previous descriptions of differences in firing rate between Purkinje cells in zebrin-positive and zebrin-negative regions (Zhou et al., 2014), and the diverse intrinsic input-output relationships in different lobules (C.H. Kim et al., 2012a).It was previously known that mGluR1 blockade can reduce Purkinje cell firing frequency (Yamakawa and Hirano, 1999) and TRPC3 perturbation can affect Purkinje cell firing rate (Sekerková et al., 2013) in a zebrin-dependent manner (Zhou et al., 2014), although the underlying mechanisms remain unclear.
The high-frequency spontaneous firing of Purkinje cells encodes the output of the cerebellar cortex and provides tonic inhibition to downstream cells in the deep cerebellar and vestibular nuclei.Consequently, the impact of homogeneous or diversified slow current timings, such as we observe in lobules IV/V versus lobule X and the flocculus, is that it could affect the synchrony or lack thereof of Purkinje cells that are activated by the same PF beam.As a result, time-locked spiking of downstream deep cerebellar nucleus (DCN) neurons may be affected, as well as a direct impact on the firing rate of DCN neurons (Telgkamp and Raman, 2002;Person and Raman, 2012;Sedaghat-Nejad et al., 2022).

Future directions
Our results highlight the importance of synaptic heterogeneity in Purkinje cell timing, which opens new areas of inquiry into how cerebellar circuits utilize this diversity.Our findings also expand the repertoire of synaptic and cellular mechanisms that different regions of the cerebellum may draw on to support diverse functions.Finally, although we did not causally link mGluR1-TRPC3 signaling to this diversity, we reveal tight and suggestive correlations with key molecular players, which provides a firm foundation for future mechanistic studies into the role of synaptic heterogeneity in Purkinje cell timing.Thus, our study is not a final verdict on Purkinje cell timing diversity but rather a key first step.

Figure 1 .
Figure1.The slow EPSC (sEPSC) was heterogenous across cerebellar lobules.a, Schematic representation of a mouse brain highlighting the recorded regions: the cerebellar flocculus and vermis.Parasagittal acute cerebellum slices were used for recordings in vermis lobules IV/V and X, while coronal sections were used for flocculus recordings.b, Representative sEPSC traces depict a delayed time of peak in lobule X and the flocculus compared with lobules IV/V.Scale bar, 100 pA, 500 ms.c, Peak amplitudes of sEPSCs were similar across lobules.*p < 0.05, Kruskal-Wallis analysis of variance on ranks followed by Dunn's multiple-comparisons test.d, sEPSC time of peak was earlier in lobules IV/V in comparison with lobule X and the flocculus.Kruskal-Wallis analysis of variance on ranks followed by Dunn's multiple-comparisons test (****p < 0.0001).e, High heterogeneity in the time of peak within lobule X and the flocculus compared with lobules IV/V is demonstrated by higher coefficients of variation.f, Lobule X sEPSCs exhibited the longest 90-10% decay time.Both lobule X and flocculus sEPSCs had longer decay times than those from lobules IV/V.*p < 0.05, ****p < 0.0001, Kruskal-Wallis analysis of variance on ranks followed by Dunn's multiple-comparisons test.g, A longer half-width sEPSC was observed in lobule X and the flocculus compared with lobules IV/V (****p < 0.0001, Kruskal-Wallis analysis of variance on ranks followed by Dunn's multiple-comparisons test).h, sEPSCs with similar peak amplitudes in lobules IV/V, lobule X, and the flocculus had different times of peak.Bubble size represents the decay time of the sEPSC.Data from each lobule were fit in an assumption-free manner with a spline in equivalent color.Violin plots show median and quartiles.(c-f, h: lobules IV/V = 56 cells from 41 mice, lobule X = 35 cells from 27 mice, flocculus = 23 cells from 14 mice.g: lobules IV/ V = 42 cells from 33 mice, lobule X = 33 cells from 26 mice, flocculus = 23 cells from 14 mice).Please refer to Extended Data Figures1-1-1-3 for further information.Additional details on statistics are presented in Materials and Methods and Extended Data Table1.

Figure 2 .
Figure 2. Zebrin/aldolase C expression did not predict sEPSC peak latency.a, Stitched sagittal sections of the mouse vermis, immunolabelled with anti-calbindin (which marks all Purkinje cells) and anti-zebrin antibodies.Rightmost panel, merged.Single arrowhead marks lobule X, double arrowhead marks lobules IV/V.Scale bar, 500 µm.b, Stitched coronal sections of the mouse cerebellum, immunolabelled with anti-calbindin and anti-zebrin antibodies.Rightmost panel, Merged.The single arrowhead marks the flocculus.Scale bar, 500 µm.c, Inset illustrates zebrin stripes.d, Zebrin-negative Purkinje cells in lobules IV/V and zebrin-positive Purkinje cells in lobule X and the flocculus.Scale bar, 100 µm.Images are maximum intensity projections of confocal stacks.e, Representative image of a 300-µm-thick cerebellar section with the Alexa Fluor 488 dye-filled Purkinje cell, with the section retrospectively stained with anti-zebrin antibody.The top row demonstrates a dye-filled cell that is zebrin-positive, and the bottom row demonstrates one that is zebrin-negative.Images are maximum intensity projections of confocal stacks.Scale bar, 100 µm.f, Schematic representing dye-fill of the whole-cell patch-clamped Purkinje cell from which sEPSCs were measured, followed by immunolabelling with anti-zebrin antibody.g, Zebrin identity did not predict the time of peak of sEPSC, across regions.Most dye-filled lobules IV/V cells were zebrin-negative (black hollow circles), and most dye-filled lobule X and flocculus

Figure 3 .
Figure3.sEPSC heterogeneity did not depend on the number of PF stimulations.a-c, Peak amplitude of sEPCS were similar in lobules IV/V, lobule X, and the flocculus in response to three, four, and five PF stimulations, respectively at 100 Hz. d-f, sEPSC time of peak was faster in lobules IV/V in response to three, four, or five PF stimulations at 100 Hz. g-i, sEPSC decay time was longer in lobule X than lobules IV/V in response to three PF stimulations at 100 Hz and longer in lobule X in comparison with both lobules IV/V and the flocculus in response to four or five PF stimulations at 100 Hz.Statistical comparisons: (b, e, f, h) *p < 0.05, **p < 0.01, ****p < 0.0001, ordinary one-way ANOVA followed by Tukey's multiple-comparison test.a, c, d, g, i, *p < 0.05, **p < 0.01, ***p < 0.001, Kruskal-Wallis test followed by Dunn's multiple-comparisons test.Violin plots show median and quartiles.(a, d, g: lobules IV/V = 3 cells from 3 mice, lobule X = 8 cells from 3 mice, flocculus = 5 cells from 2 mice.b, e, h: lobules IV/V = 5 cells from 3 mice, lobule X = 7 cells from 3 mice, flocculus = 10 cells from 5 mice.c, f, i: lobules IV/V = 5 cells from 3 mice, lobule X = 7 cells from 3 mice; flocculus = 11 cells from 5 mice).Additional details on statistics are in Extended Data Table1.

Figure 8 .
Figure 8. TRPC3 to mGluR1a ratio was higher in lobules IV/V, but mGluR1 and TRPC3 localization was the same across lobules.a, b, Antibody staining for calbindin, mGluR1a, and TRPC3 on 50-µm-thick cerebellar sections demonstrates similar cellular localization across lobules.Scale bars: a, 100 µm; b, 50 µm.c, Mean fluorescence intensities of TRPC3 and mGluR1a were measured in the molecular layer of each lobule, the background intensity was subtracted, and the ratio of TRPC3 to mGluR1 was determined.Each data point is one region from one brain section.For each region (lobules IV/V, lobule X, flocculus), there are two sections per mouse and four mice per region.One-way ANOVA followed by Tukey's multiple-comparisons test, ****p < 0.0001.

Figure 9 .
Figure 9. sEPSC heterogeneity diversifies Purkinje cell spike timing.a-c, sEPSC traces in response to 10 PF stimulations at 100 Hz recorded from Purkinje cells voltage-clamped at −70 mV.Scale bar 100 pA, 250 ms.d-f, Mean spike counts binned into 100 ms time bins from the same Purkinje cells, spiking in current-clamp conditions, in response to the same stimulation of 10PF stimulations at 100 Hz. g-i, Overlay of 100 ms time-binned mean spike counts from the same Purkinje cells under current-clamp conditions in response to 10PF stimulations at (g) 50 Hz, (h) 100 Hz, and (i) 150 Hz. j, Top, Representative trace of a cell-attached recording from lobules IV/V, with PF stimulation at time 0 and 10 stimulus pulses at 100 Hz.Bottom, Normalized instantaneous spike frequency binned into 100 ms time bins.The representative cell-attached trace is aligned in time to the x-axis of the graph.k, l, Same as in j but for lobule X and the flocculus, respectively.All data are mean ± SEM. (a-i: lobules IV/V = 4 cells from 4 mice, lobule X = 8 cells from 8 mice, flocculus = 5 cells from 4 mice; j-l: lobules IV/V = 11 cells from 4 mice, lobule X = 8 cells from 3 mice, flocculus = 9 cells from 3 mice).

Figure 10 .
Figure10.There is heterogeneity in parallel fiber-driven Purkinje cell firing even when fast synaptic transmission was not blocked.a-c, Top, Representative trace of cell-attached recordings, where 0 marks the time of five PF stimulations at 100 Hz.Bottom, Normalized spike frequency binned into 100 ms bins for (a) lobules IV/V, (b) lobule X, and (c) the flocculus.These recordings did not contain NBQX or picrotoxin, and therefore fast excitatory and inhibitory synaptic transmission were intact.(Lobules IV/V = 13 cells from 5 mice, lobule X = 9 cells from 4 mice, flocculus = 10 cells from 3 mice).